摘要:
Tissue plasminogen activator analogs exhibiting greater specificity for fibrin than native t-PA are disclosed. The analogs include the K1 domain of native t-PA replaced with another kringle domain mediating the binding of the analog to fibrin. The kringle contains six cysteine residues. The t-PA analogs may further include a variety of substitutions and modifications. Pharmaceutical compositions containing one or more of the t-PA analogs along with a physiologically acceptable carrier or diluent are also disclosed.
摘要:
Tissue plasminogen activator analogs containing the growth factor domain of native t-PA, the domain having at least one cysteine residue replaced with another amino acid. The t-PA analogs may further contain a variety of substitutions and/or modifications. Pharmaceutical compositions containing one or more of the t-PA analogs along with a physiologically acceptable carrier or diluent are also disclosed.
摘要:
Tissue plasminogen activator analogs containing the growth factor domain of native t-PA, the domain having at least one cysteine residue replaced with another amino acid. The t-PA analogs may further contain a variety of substitutions and/or modifications. Pharmaceutical compositions containing one or more of the t-PA analogs along with a physiologically acceptable carrier or diluent are also disclosed.
摘要:
A coated ubidecarenone-containing liposome which comprises the ubidecarenone-containing liposome and a polysccharide fatty acid ester applied on the surface of membrane of said liposome, whereby the ubidecarenone can be selectively and richly transferred to the lungs, spleen and kidneys.
摘要:
A ubidecarenone-containing liposome is provided which permits ubidecarenone to be transferred to a target organ at an increased speed. There is also disclosed a pharmaceutical composition containing the ubidecarenone-containing liposome acc. to the invention.
摘要:
A ubidecarenone-containing liposome is provided which permits ubidecarenone to be transferred to a target organ at an increased speed. There is also disclosed a pharmaceutical composition containing the ubidecarenone-containing liposome acc. to the invention.